29 - 30 November, 2023
Ensure Trial Success Through Building Effective Partnerships and Implementing Strong Outsourcing Strategies
Collaborate and Achieve Goals with Expert Guidance from Leading Stakeholder Perspectives
Providing a thorough overview of partnership and outsourcing strategy, regulatory updates, RWE and data privacy
Explore the Essential Updates with Panel Discussions, Live Q&As, Case Studies and more
Latest Learnings with Real World Evidence:
- Hear a joint presentation on Real World Data in Practice- Perspectives from the MHRA and a Clinician
- Examples of Real World Data and evidence and how it was implemented
- AstraZeneca will discuss how they developed a quality management checklist to support audits of Real-World Data (RWD) used in regulatory submissions.
- Participate in an interactive discussion addressing: Real World Evidence – Experiences
Partnership, Outsourcing, Regulatory Updates and Data Privacy:
- Hear a Case Study from GSK’s on FSP Partnership, Critical Factors for FSP Transition of Sponsor Studies
- Join the debate - What does long term partnerships really mean?
- Regulatory best practices of the clinical trial regulation and the accelerated clinical trials in EU, HMA, EMA and EU commission initiative
- Learnings on the impact and industry perspective for EU Clinical Trial Regulation 536/2014 from Seagen